| Geno
|
Mag
|
Summary
|
| (A;A)
|
0
|
|
| (C;C)
|
2
|
>1.26x increased risk for heart disease
|
| (C;T)
|
|
1.26x increased risk for heart disease
|
| (T;T)
|
0
|
normal
|
| ? | (C;C) (C;T) (T;T) | 28 |
 |
rs17228212 is a SNP found to be associated with
heart disease by the German MI (Myocardial infarction) Family Study group in two populations. The odds ratio per allele is 1.26 (CI: 1.11-1.44, p=0.0178).[
PMID 17634449]
[PMID 18979498] rs599839, rs4970834 and rs17228212 associated with non-HDL cholesterol
[PMID 18780302] Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.
[PMID 19198609] Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
[PMID 19750184] Genome-wide association studies for atherosclerotic vascular disease and its risk factors.
[PMID 19956433] Genetics of coronary artery disease: focus on genome-wide association studies.
[PMID 20017983] Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.
[PMID 20098575] Genetics and cardiovascular disease: Design and development of a DNA biobank.
[PMID 21804106] Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.
| GET Evidence
|
| rs17228212
|
| aa_change
|
|
| aa_change_short
|
|
| impact
|
pathogenic
|
| qualified_impact
|
Insufficiently evaluated pathogenic
|
| overall_frequency
|
0.1875
|
| summary
|
|